(2S,4S)-Methyl 1-((S)-2-((Tert-Butoxycarbonyl)Amino)-3,3-Dimethylbutanoyl)-4-Hydroxypyrrolidine-2-Carboxylate

98%

Reagent Code: #237314
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CAS Number 817183-32-7

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 358.43 g/mol
Formula C₁₇H₃₀N₂O₆
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Widely used in peptide synthesis and medicinal chemistry as a chiral building block, this compound serves as a key intermediate in the preparation of protease inhibitors, particularly for viral targets such as hepatitis C virus (HCV) NS3/4A protease. Its stereochemistry allows for high selectivity in asymmetric reactions, making it valuable in the development of active pharmaceutical ingredients (APIs) requiring precise 3D configuration. The presence of protected functional groups enables stepwise coupling and deprotection strategies in solid-phase and solution-phase synthesis. It is especially useful in constructing complex molecules where steric control and functional group compatibility are critical.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,090.00
inventory 250mg
10-20 days ฿33,480.00
inventory 1g
10-20 days ฿82,180.00
(2S,4S)-Methyl 1-((S)-2-((Tert-Butoxycarbonyl)Amino)-3,3-Dimethylbutanoyl)-4-Hydroxypyrrolidine-2-Carboxylate
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Widely used in peptide synthesis and medicinal chemistry as a chiral building block, this compound serves as a key intermediate in the preparation of protease inhibitors, particularly for viral targets such as hepatitis C virus (HCV) NS3/4A protease. Its stereochemistry allows for high selectivity in asymmetric reactions, making it valuable in the development of active pharmaceutical ingredients (APIs) requiring precise 3D configuration. The presence of protected functional groups enables stepwise coupli

Widely used in peptide synthesis and medicinal chemistry as a chiral building block, this compound serves as a key intermediate in the preparation of protease inhibitors, particularly for viral targets such as hepatitis C virus (HCV) NS3/4A protease. Its stereochemistry allows for high selectivity in asymmetric reactions, making it valuable in the development of active pharmaceutical ingredients (APIs) requiring precise 3D configuration. The presence of protected functional groups enables stepwise coupling and deprotection strategies in solid-phase and solution-phase synthesis. It is especially useful in constructing complex molecules where steric control and functional group compatibility are critical.

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